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FDA recall record

Strawberry, Kiwi, Blueberry packaged in the following sizes and brands: 1. Item 80846. Net Wt. 12 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store bran...

Recall F-1762-2022Class IITerminatedJuly 29, 2022

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of September 23, 2022. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Strawberry, Kiwi, Blueberry packaged in the following sizes and brands: 1. Item 80846. Net Wt. 12 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded. 2. Item 80865. Net Wt. 20 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded.

Reason

Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Strawberry, Kiwi, Blueberry packaged in the following sizes and brands: 1. Item 80846. Net Wt. 12 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded. 2. Item 80865. Net Wt. 20 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded.

Code information listed by FDA

1. Lot Code: X5940967, X5943116, X5945409, X5948160, X5950862, X5955338, X5957066, X5959530, X5962259, X5964838, X5967661, X5972168, X5974141, X5976428, X5979127, X5981797, X5984467, X5989189, X5987083, X5993374, X5995963, X5998561. Use by Dates: 7/9-8/2/2022 2.

Lot Code: X5940980, X5943138, X5943138, X5945421, X5948178, X5950877, X5955350, X5950877, X5957083, X5959716, X5962271, X5964851, X5967678, X5972177, X5974154, X5976478, X5979138, X5981808, X5984481, X5989197, X5990976, X5993384, X5996070, X5998688. Use by Dates: 7/9-8/2/2022

Distribution and firm information

Recalling firm listed by FDA: Russ Davis Wholesale, LLC

Firm location listed by FDA: Inver Grove Heights, MN, United States

Distribution reported by FDA: IA, MI, MN, ND, SD, WI

Product quantity listed by FDA: 87,915 units total

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.